| Tag | Content |
|---|
EnhancerAtlas ID | HS059-38790 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr5:176431880-176433280 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr5:176432472-176432482 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr5:176432472-176432482 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr5:176432472-176432482 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_60845 | chr5:176411918-176434682 | DHL6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACTTTTACCC CTAAATAGGT ACCTAGCACT TTCTTTATTT GGAGACAAGG TCTTGCTCTG 60
TCACCCAGGC TGGAGTGCAG TAGGGCAATC AGCCTCGACC TGGTCCAAAG GTCAAGCAAT 120
CCTCCTACCT CAGTTTCCCG AGAAGCTGGG AACCACAGGC ACGCGCCACC ACGCCCAGCT 180
AATTTTTTTT TTTTAATTTT GAGGGTTTTA AGAGACAGGG TCTCACTCTC TTGCCCATGC 240
TGAAGGGCAG TGGCACGATC ATAGCTCACC TGCAGCCTCC ACTTCCTGGG CTCACGGGAT 300
CCTCCTGCCT CAGCCACCTG AGTAGCTGAG ACTATAGGCA GGCGCCACCA CACTCTAATA 360
ATTTTTTTTA TTTTTTGTAG AGACAGGGTC TCCTATGTTG CCCAGGCGGG TCTTGATACT 420
CCTGGACTCA AGTGATTTTT CTGCCTCGGC CTCTCAAAGT GCTGGGAGTA TAGGAGTGAG 480
CCACCAGGCC CGTCGACCAA GCGCTCTAAT AACTAAATAC AATGAACTTA TTTCCGTAAT 540
TTTTGTAAAA AGGTAAATGC ATACCTACAC ACGCATACAT CCCTGATACT TCATTTTCCA 600
TTTTTTCAGT TTATATTCAG CCTCAGTTTA GGACAAGTGT GTAACAATAC AATCCAAACA 660
CTTTAGTATC TAGTATCACA ACAACTCTGC GTCGTAGGTA TTCATATCAC GATGTTCCAC 720
ATGAGGAAAC TTAACGCAAA CAGCGGATAA GCTGGTAAAG GGCTGAGAGT TGAAGCTGAA 780
TGTATCTGAT TCCAAAAACA CACTTTCATT CGACTACAAG GCACTGCCTC CCTTGACAGG 840
AAAACAATAA AGACAGAAGC ATAAACTTTT CACTTTTTCC GGGTGTCATT TCTATATCTC 900
GGTGCGATGT AGTGATTAAA TGAAAGAACA CTGGAGTCCA GCTGCTGGGA TTCAAATCCA 960
GCTCCACTAC TGCCCGGGAC TCGCGCCCCG TTAACTGAGC GGCAGGGCAC CAGCCCGCCG 1020
GCTGTGGCGC TCGAGAAGCC TGCGGCGCTG CCTAAGCACC TGGAAACGCG CCGGCCCTGC 1080
GGGGGCGAAA TCGTCTAGGA CGATAGGGAT CTCCAAGGAG TGCGCTGGGG GTTATTTTCG 1140
GGGCAAATAA TTAGAGAAAA CGAGGATCAC ACAACAAAAC AGCAACCCGG CACGGGAAGG 1200
AGCGCGGGCC TGGCGCCCCG AGGCGTGAGG CGGCGCGGAC CACGGCTGAG GGAGCTCGGC 1260
GCTCGCCCGA CGCCCGGGAG GATGCAGGCC GCCCCCCAGG TGTGAAAGGG ACCCGCCCGG 1320
CAACCGAAGG TGCAAAGCCC AACCTGGCGT TCCGAGGGGC CCTGCGTGGC GTCAGGGGAG 1380
ACCCAACCCG CGTCCCGAAC 1400
|
